Evidence map›Paper›PMID 20081808›Full record

ArticleModern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc2010

Carbonic anhydrase II. A novel biomarker for gastrointestinal stromal tumors.

Seppo Parkkila, Jerzy Lasota, Jonathan A Fletcher, Wen-Bin Ou, Antti J Kivelä, Kyösti Nuorva, Anna-Kaisa Parkkila, Jyrki Ollikainen, William S Sly, Abdul Waheed and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
6.6field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

42 citing papers in PubMed, 99 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Proton Transport in Cancer Cells: The Role of Carbonic Anhydrases.International journal of molecular sciences · 2021
    Review
  13. Review
  14. Review
  15. Review
  16. Article
  17. Review
  18. Carbonic anhydrases as disease markers.Expert opinion on therapeutic patents · 2019
    Review
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 8 institutions in 3 countries.

Seppo ParkkilaDepartment of Anatomy, University of Tampere and Tampere University Hospital, Tampere, Finland. Seppo.Parkkila@uta.fi
Jerzy Lasota
Jonathan A Fletcher
Wen-Bin Ou
Antti J Kivelä
Kyösti Nuorva
Anna-Kaisa Parkkila
Jyrki Ollikainen
William S Sly
Abdul Waheed
Silvia Pastorekova
Jaromir Pastorek
Jorma Isola
Markku Miettinen
Tampere University · FIArmed Forces Institute of Pathology · USCentral Finland Health Care District · FISaint Louis University · USSlovak Academy of Sciences · SKBrigham and Women's Hospital · USHarvard University · USTampere University · FI

Funding

Tissue and Pathology ResourcesP50CA127003 · NCI · DANA-FARBER CANCER INST · PI EL-BARDEESY, NABEEL, SELLERS, WILLIAM R · 2007 to 2023
$33.2M
NCI NIH HHS P50 CA127003
6 · The paper itself

Abstract

Gastrointestinal stromal tumors (GISTs) are clinically distinct mesenchymal tumors, which generally result from expression of mutant KIT or PDGFRA receptor tyrosine kinase oncogenes. Most GISTs feature strong expression of KIT that serves as a crucial diagnostic adjunct. However, a subset of tumors lacks KIT expression and otherwise may also be difficult to distinguish from other sarcomas, including leiomyosarcoma. Because various carbonic anhydrase (CA) isozymes have been identified as potential treatment targets against different cancers, we evaluated CA II expression in 175 GISTs. Western blotting experiments indicated that CA II is highly expressed in GIST cell lines. Immunohistochemically, 95% of GISTs showed positive signal. The CA II expression in GISTs did not correlate with particular KIT or PDGFRA mutation types. CA II immunoreactivity was absent or low in other mesenchymal tumor categories analyzed. High CA II expression was associated with a better disease-specific survival rate than low or no expression (Mantel-Cox test, P<0.0001). The present results indicate that CA II is overexpressed in most GISTs, is quite selective to this tumor type among mesenchymal tumors, and therefore might be a useful biomarker in diagnostics.

Indexed as

Biomarkers, TumorBlotting, WesternCarbonic Anhydrase IIGastrointestinal Stromal TumorsHumansImmunohistochemistryIntestinal NeoplasmsIntestine, SmallStomach NeoplasmsBiomarkers, TumorCarbonic Anhydrase II

Identifiers

PMID20081808
PMCPMC2900582
OpenAlexW2102715786

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.